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Volumn 4, Issue 5, 2002, Pages 675-678

Stereoselective ring expansion via bicyclooxonium ion. A novel approach to oxocanes

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EID: 0001739666     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016919k     Document Type: Article
Times cited : (17)

References (32)
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    • For reviews, see: (a) Shimizu, Y. Chem. Rev. 1993, 93, 1685.
    • (1993) Chem. Rev. , vol.93 , pp. 1685
    • Shimizu, Y.1
  • 3
    • 0002144535 scopus 로고
    • Scheuer, P. J., Ed.; Academic Press: New York
    • For reviews, see: (a) Moore, R. E. In Marine Natural Products; Scheuer, P. J., Ed.; Academic Press: New York, 1978; Vol. 1, pp 43-121.
    • (1978) Marine Natural Products , vol.1 , pp. 43-121
    • Moore, R.E.1
  • 4
    • 0000359232 scopus 로고
    • Scheuer, P. J., Ed.; Academic Press: New York
    • (b) Erickson, K. L. In Marine Natural Products; Scheuer, P. J., Ed.; Academic Press: New York, 1983; Vol V, pp 131-257.
    • (1983) Marine Natural Products , vol.5 , pp. 131-257
    • Erickson, K.L.1
  • 5
    • 0035137292 scopus 로고    scopus 로고
    • (c) Faulkner, D. J. Nat. Prod. Rep. 2001, 18, 1. See also his previous reviews in Nat. Prod. Rep.
    • (2001) Nat. Prod. Rep. , vol.18 , pp. 1
    • Faulkner, D.J.1
  • 6
    • 0035137292 scopus 로고    scopus 로고
    • (c) Faulkner, D. J. Nat. Prod. Rep. 2001, 18, 1. See also his previous reviews in Nat. Prod. Rep.
    • Nat. Prod. Rep.
  • 17
    • 0030489899 scopus 로고    scopus 로고
    • 1,4-and 1,5-Rearrangement-ring expansion of oxiranes via bicyclo-[3.1.0] and [4.1.0]oxonium ions, respectively, were reported, (a) Hayashi, N.; Fujiwara, K.; Murai, A. Chem. Lett. 1996, 341.
    • (1996) Chem. Lett. , pp. 341
    • Hayashi, N.1    Fujiwara, K.2    Murai, A.3
  • 29
    • 85034523626 scopus 로고    scopus 로고
    • 2 at 0°C. See ref 12 for preparation of 10b
    • 2 at 0°C. See ref 12 for preparation of 10b.
  • 31
    • 85034523721 scopus 로고    scopus 로고
    • note
    • 3) δ 74.3, 71.7, 33.9, 32.7, 22.0.
  • 32
    • 85034525782 scopus 로고    scopus 로고
    • 1H NMR spectrum analysis of the diastereomeric mixture of their (R)-MTPA ester derivatives. This result indicates that 23b was produced via meso-bicyclooxonium ion intermediate 22
    • 1H NMR spectrum analysis of the diastereomeric mixture of their (R)-MTPA ester derivatives. This result indicates that 23b was produced via meso-bicyclooxonium ion intermediate 22.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.